Dr. Andreas Hentschel

Journal of Neuropathology and Experimental Neurology, 2026

Kolbel H, Hentschel A, Preusse C, Tiet M, Dohrn MF, Muhmann D, van den Ameele J, Chen L, Schara-Schmidt U, Weis J, Horvath R, Mensch A, Roos A.

When muscles matter in SORD neuropathy

Biomolecules, Vol. 16, No. 7, 2026

Holland SH, Carmona-Martinez R, Hentschel A, Derksen A, O'Connor K, O'Neil D, Ho K, Baird SD, Roos A, Spendiff S, Lochmuller H.

Hexosamine Pathway Disruption by GFPT1 Loss Drives Coordinated Defects in Glycosylation, Autophagy, and Trafficking

Gene Therapy, Vol. 2026, 2026

Georgiou E, Kagiava A, Hentschel A, Sargiannidou I, Papacharalampous R, Stavrou M, Tryfonos C, Richter J, Roos A, Kleopa KA.

A dose-escalation and safety gene therapy study in a model of CMT4C neuropathy

Acta Neuropathologica, Vol. 151, No. 1, 2026

Kleefeld F, Teran Gamboa J, Pinal-Fernandez I, Preusse C, Nelke C, Goebel H, Mensch A, Mossakowski A, Miah M, Diaz-Manera J, Torchia E, Bortolani S,…

Brachio-cervical inflammatory myopathy: multilevel clinical, histopathological and multi-omic analyses of a syndrome variably associated with systemic sclerosis

Communications Biology, Vol. 9, No. 1, 2026

Bertino F, Zanin Venturini DI, Grasso E, Kopecka J, Salio C, Gnutti B, Basnet RM, Bellini S, Mignani L, Zhao B, Kleefeld F, Hentschel A, Magnani F,…

Mitochondrial energetic failure underlies FLVCR1-related sensory neuropathy

Skeletal Muscle, Vol. 16, No. 1, 2026, P. 1-18

Daya NM, Schänzer A, Hentschel A, Kienitz M, Sellung D, Suedkamp N, Krause K, Kinold JC, Volke L, Schreiner A, Schlierbach H, Nelke C, Kleefeld F,…

Unveiling FLNC variants: iPSC-derived myogenic cells as a model to study disease mechanisms

Journal of Neurology, Vol. 273, No. 2, 2026, P. 94

Mroczek M, Preusse C, Hentschel A, Chroscinska-Krawczyk M, Bielak M, Sobolewska A, Della Marina A, Hila A, Iyadurai S, Kraft F, Chetty VK, Muhmann D,…

Exploring molecular signatures in PURA syndrome using muscle proteomics and serum biomarkers

Clinical Genetics, Vol. 109, No. 5, 2026, P. 978-983

Kilicarslan OA, Gangfuß A, Hentschel A, Koelbel H, Muhmann D, Töpf A, Stöhr M, Chen L, Horvath R, Thompson R, Schara-Schmidt U, Kurth I, Lochmüller…

A Homozygous CPSF1 Variant Causes Congenital Cataract, Intellectual Disability and Hyperphagia

Journal of Clinical Medicine, Vol. 14, No. 24, 2025

Aksel Kilicarslan O, Gangfuss A, Kolbel H, Muhmann D, Polavarapu K, Thompson R, Schmitt L, Lessard L, Chen L, Eisenkolbl A, Schara-Schmidt U,…

Combined Histological and Proteomic Analysis Reveals Muscle Denervation in KMT5B-Related Neurodevelopmental Disorder: A Case Report

Journal of Proteome Research, Vol. 2025, 2025, P. 484-490

Lange E, Schallert K, Schwerdt J, Ghosh S, Hentschel A, Reinders Y, Heyer R.

The Omics Molecule Extractor: A Web Application for the Selection of Potential Biomarker Panels